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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961130copy number variation1nstd209human GRCh38 chr22: 27,221,188-27,221,323 , GRCh37.p13 chr22: 27,617,149-27,617,284 LINC01638
    nsv5960367copy number variation1nstd209human GRCh38 chr22: 27,219,323-27,220,851 , GRCh37.p13 chr22: 27,615,284-27,616,812 LINC01638
    nsv5872483copy number variation1nstd209human GRCh38 chr22: 27,219,334-27,220,895 , GRCh37.p13 chr22: 27,615,295-27,616,856 LINC01638
    nsv5596006copy number variation1nstd207human GRCh38 chr22: 27,221,193-27,221,332 , GRCh37.p13 chr22: 27,617,154-27,617,293 LINC01638
    nsv5553292copy number variation1nstd206human GRCh38 chr22: 27,221,185-27,221,327 , GRCh37.p13 chr22: 27,617,146-27,617,288 LINC01638
    nsv5322890copy number variation1nstd204human GRCh38.p13 chr22: 27,221,197-27,221,313 , GRCh37.p13 chr22: 27,617,158-27,617,274 LINC01638
    nsv5033059copy number variation1nstd200human GRCh38 chr22: 27,089,956-27,381,938 , GRCh37.p13 chr22: 27,485,918-27,777,899 LOC105372977, LOC107985534, 4 more genes
    nsv5031423copy number variation1nstd200human GRCh38 chr22: 27,220,422-27,226,973 , GRCh37.p13 chr22: 27,616,383-27,622,934 LINC01638
    nsv4869287copy number variation1nstd200human GRCh37 chr22: 27,616,383-27,622,934 , GRCh38.p12 chr22: 27,220,422-27,226,973 LINC01638
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676280copy number variation1nstd102humanPathogenic GRCh37 chr22: 26,337,910-28,489,947 , GRCh38.p12 chr22: 25,941,943-28,093,959 LOC646216, MYO18B, 42 more genes
    nsv4676144copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-27,657,507 , GRCh38.p12 chr22: 16,408,173-27,261,546 LINC02891, IGLV4-69, 466 more genes
    nsv4641505copy number variation2nstd186human GRCh37 chr22: 27,617,167-27,617,266 , GRCh38.p12 chr22: 27,221,206-27,221,305 LINC01638
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4426402copy number variation1nstd174human GRCh37 chr22: 27,617,047-27,617,270 , GRCh38.p12 chr22: 27,221,086-27,221,309 LINC01638
    nsv4383389copy number variation1nstd173human GRCh37 chr22: 21,465,662-33,984,045 , GRCh38.p12 chr22: 21,111,373-33,588,059 , XBP1, 450 more genes
    nsv4316382inversion1nstd166human GRCh37.p13 chr22: 22,466,414-30,881,792 , GRCh38.p12 chr22: 22,112,004-30,485,805 , CRYBB2, 313 more genes
    nsv4290367copy number variation1nstd166human GRCh37.p13 chr22: 27,617,167-27,617,266 , GRCh38.p12 chr22: 27,221,206-27,221,305 LINC01638
    nsv3924941copy number variation1nstd102humanPathogenic GRCh38 chr22: 26,221,273-29,477,543 , GRCh37 chr22: 26,617,239-29,873,532 , NCBI36 chr22: 24,947,239-28,203,532 TFIP11, RASL10A, 66 more genes
    nsv3923205copy number variation1nstd102humanPathogenic NCBI36 chr22: 25,177,008-30,177,912 , GRCh37 chr22: 26,847,008-31,847,912 , GRCh38 chr22: 26,451,042-31,451,926 DRG1, THOC5, 138 more genes
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